Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1275325035
Device Listing 1275325035
Listing Summary
#
Listing key
1275325035
Premarket submission
K022384
Device
XENON FIBEROPTIC LIGHT SOURCE, MODEL 1300 XSBP
Applicant
Isolux America
Product code
HET
Decision date
2002-10-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
22641
1064515
3002249830
ISOLUX LLC
1
N
2020-04-25
1045 COLLIER CENTER WAY SUITE No. 6 NAPLES FL US 34110